Package 0574-0150-04

Brand: midazolam hydrochloride

Generic: midazolam hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0574-0150-04
Digits Only 0574015004
Product NDC 0574-0150
Description

1 BOTTLE, GLASS in 1 CARTON (0574-0150-04) / 118 mL in 1 BOTTLE, GLASS

Marketing

Marketing Status
Marketed Since 2005-05-02
Brand midazolam hydrochloride
Generic midazolam hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d7b8dd9f-1acd-4d10-afbf-a57a93154a6b", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["422410"], "spl_set_id": ["0be63f63-6a93-4782-8f9c-d13ca5ae44bd"], "manufacturer_name": ["Padagis US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (0574-0150-04)  / 118 mL in 1 BOTTLE, GLASS", "package_ndc": "0574-0150-04", "marketing_start_date": "20050502"}], "brand_name": "Midazolam Hydrochloride", "product_id": "0574-0150_d7b8dd9f-1acd-4d10-afbf-a57a93154a6b", "dosage_form": "SYRUP", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0574-0150", "dea_schedule": "CIV", "generic_name": "Midazolam Hydrochloride", "labeler_name": "Padagis US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midazolam Hydrochloride", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA076379", "marketing_category": "ANDA", "marketing_start_date": "20050502", "listing_expiration_date": "20261231"}